Page 287 - Proceeding The 2nd International Seminar of Science and Technology : Accelerating Sustainable Innovation Towards Society 5.0
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nd
               The 2  International Seminar of Science and Technology
               “Accelerating Sustainable innovation towards Society 5.0”
               ISST 2022 FST UT 2022
               Universitas Terbuka
               d.  Spermatozoa Morphology
                   Spermatozoa  morphology  was  tested  using  eosin-nigrosine
                   staining. The procedure for making preparations is the same as
                   that  for  observing  spermatoza  viability.  The  preparations  were
                   observed  under  a  microscope  with  a  magnification  of  40  ×  10.
                   Spermatozoa were observed in 10 fields of view or with a sperm
                   count of at least 200 cells. Spermatozoa morphology testing was
                   conducted to see the normality and abnormality of spermatozoa.
                   Spermatozoa were counted by dividing the number of abnormal
                   spermatozoa  by  the  total  number  of  spermatozoa  counted
                   multiplied by 100%, with Equation (2):
                    Spermatozoa abnormality =                             (2
                    Σ abnormal spermatozoa                                 )
                                            × 100%
                      Σ total spermatozoa
               2.7   Semen Processing
               Semen/spermatozoa are mixed with diluent. Dilution can be calculated
               by  the  following  equation  (3),  where  V  =  Semen  volume  (ml),  M  =
               Spermatozoa  motility  (%),  K  =  Spermatozoa  concentration
               (million/ml), IB dose = 25 million.
                                     V × M × K                           (3)
                Dilution volume (ml) =         × 0.25
                                      IB dose
               2.8   Freezing and Spermatozoa Quality Testing after Freezing
               Semen was packed in mini straws (0.25 ml) and then equilibrated at 5
               °C  for  four  hours.  The  freezing  process  was  carried  out  using
               Styrofoam measuring 38 × 27 × 27 by storing a 6 cm high straw rack
               of  liquid  nitrogen  (evaporated)  for  ten  minutes.  Frozen  semen  was
                                          o
               stored in liquid nitrogen (-196 C) for evaluation. The parameters of
               frozen semen examination include motility, viability, the same as in
               fresh  semen.  Furthermore,  several  attributes  of  the  ecological
               dimensions of the utilization of epididymal spermatozoa are discussed
               using  the  DELPHI method, using controlled,  iterative  and feedback
               information  collection.  To  determine  the  leverage  factors  and  the
               sustainability status of the ecological dimension of the utilization of



               ISST 2022 – FST Universitas Terbuka, Indonesia            257
               International Seminar of Science and Technology “Accelerating Sustainable
               Towards Society 5.0
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